Abstract

While improved tumor treatment has significantly reduced the overall mortality rates, invasive progression including recurrence, therapy resistance and metastasis contributes to the majority of deaths caused by cancer. Enhancers are essential distal DNA regulatory elements that control temporal- or spatial-specific gene expression patterns during development and other biological processes. Genome-wide sequencing has revealed frequent alterations of enhancers in cancers and reprogramming of distal enhancers has emerged as one of the important features for tumors. In this review, we will discuss tumor progression-associated enhancer dynamics, its transcription factor (TF) drivers and how enhancer reprogramming modulates gene expression during cancer invasive progression. Additionally, we will explore recent advancements in contemporary technology including single-cell sequencing, spatial transcriptomics and CUT&RUN, which have permitted integrated studies of enhancer reprogramming in vivo. Given the essential roles of enhancer dynamics and its drivers in controlling cancer progression and treatment outcome, understanding these changes will be paramount in mitigating invasive events and discovering novel therapeutic targets.

Highlights

  • Cancer is the second leading cause of death in the United States

  • Enhancer function is one of the major drivers in many tumors, as enhancers play a major role in cell identity maintenance and cell adaption to environmental changes, and alterations in enhancer activity can subvert cell fate determination [73, 135]

  • Recent studies have indicated that reprogramming of enhancer function could lead to deregulation of gene expression profile and confer cell growth advantages, promoting cancer progression [97, 99]

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Summary

Introduction

Cancer is the second leading cause of death in the United States. Over 1.8 million new cases and over 600,000 deaths due to cancer were estimated during 2020 [1]. Functional enhancers require a number of proteins to facilitate enhanced transcription of their target genes. Besides direct binding to DNA, TFs can be recruited in trans to either activate or repress specific target genes [55,56,57].

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